Method to improve properties of polymers by blending nanoparticles with polymer material


Researchers at the Department of Energy have discovered a surprising way to improve the properties of polymers by blending nanoparticles with polymer materials, as per A team of scientists led by the DoE’s Oak Ridge National Laboratory (ORNL) were studying the role of polymer structure, the interaction between nanoparticles and polymer, and nanoparticle size and shape on the structure, dynamics, and macroscopic properties of polymer nanocomposites, which are used in numerous applications.

Understanding these effects would allow the team—which also included researchers from the University of Illinois at Urbana-Champaign (Illinois) and the University of Tennessee, Knoxville (UTK) - to improve the design of new composite polymers, since they can tune mechanical, chemical, electrical, optical and thermal properties. In particular, the team was trying to verify that shrinking the nanoparticle size would adversely affect the mechanical properties of polymer nanocomposites, but they learned something else entirely, according to Alexei Sokolov, a researcher from ORNL and UTK. “We expected that there is a limit of how small a nanoparticle should be to affect macroscopic properties of nanocomposite,” he told Design News . “And at the nanoparticle size, we expected either no effect or deterioration of nanocomposite properties. We got a surprise.”

What researchers learned instead was not that an optimal nanoparticle size must exist, which is what they believed they would discover. Instead, they found that moving to really small nanoparticles enabled them to access totally new properties, Sokolov said. This occurred not due to size but because small particles move faster than large ones and interact with fewer polymer segments on the same chain. Many more polymer segments stick to a large nanoparticle, making dissociation of a chain from that nanoparticle difficult.
“Now we realize that we can tune the mobility of the particles—how fast they can move, by changing particle size, and how strongly they will interact with the polymer, by changing their surface,” Sokolov said. “We can tune mobility of nanoparticles—e.g. their weight and size—and we can also tune the time of nanoparticle-polymer dissociation by tuning strength of their interactions.” Both of these parameters affect macroscopic properties drastically, he said. “It was not possible to tune these parameters in the required range with larger nanoparticles, and this is probably the reason nobody actually tried it earlier,” Sokolov said.

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